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Excipient
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#	Item
91	Bristol-Myers Squibb Pharmaceutical Research Institute PC) Box4000 Prmceton.NJ[removed] Add to Reading List Source URL: www.fda.gov Language: English - Date: 2003-02-26 06:56:16 Research Clinical research Drug discovery Design of experiments Food and Drug Administration Pre-clinical development Excipient Clinical trial Bioavailability Pharmaceutical sciences Pharmaceutical industry Pharmacology
92	-[removed]Summary of Quality Differences This form must be completed and submitted to each Non-EU agency proposed in the EOI Request Summary of Quality Differences Modules and numbering reflect the ICH Common Add to Reading List Source URL: www.hma.eu Language: English - Date: 2014-07-30 10:43:37 Excipient European Union Political philosophy Sociology Pharmaceutical industry Pharmacology Clinical research
93	Experience in Implementing ICH Guidelines Q1-Q7 Perspectives from Industry Workshop on Implementation of ICH Q8/Q9/Q10 and Other Quality Guidelines Presented by JCCT Co-sponsored by APEC-LSIF and ICH GCG Add to Reading List Source URL: www.ich.org Language: English - Date: 2012-06-22 04:06:30 Technology Clinical research Pharmaceutical industry Quality Food and Drug Administration United States Public Health Service Specification Packaging and labeling Excipient Medicine Pharmacology Pharmaceutical sciences
94	The Impact of Excipient Variability on QbD Add to Reading List Source URL: www.ich.org Language: English - Date: 2012-06-22 04:06:22 Food additives Carrageenan Microbicides Polysaccharides Biology Excipient Medicine Eucheuma Kappaphycus alvarezii Red algae Food and drink Pharmaceutical industry
95	CMC Considerations for a Successful Regulatory Submission Rapti D. Madurawe, Ph. D. Branch Chief Office of New Drug Quality Assessment 1 Add to Reading List Source URL: www.fda.gov Language: English Health Pharmaceutical industry Food and Drug Administration Clinical research Drug safety Investigational New Drug Clinical trial Excipient Regulatory requirement Pharmacology Pharmaceutical sciences Research
96	PDF Document Add to Reading List Source URL: www.fda.gov Language: English - Date: 2002-10-30 13:51:29 Medicine Dosage forms Clinical research Drug safety Abbreviated New Drug Application Food and Drug Administration New Drug Application Excipient Capsule Pharmaceutical sciences Pharmacology Pharmaceutical industry
97	Novartis Pharma AG Basel, Switzerland d> NOVARTIS Novartis Pharma AG Add to Reading List Source URL: www.fda.gov Language: English - Date: 2003-02-06 07:12:31 Clinical research Pharmaceutical industry Drug discovery Pharmaceuticals policy Novartis Excipient Food and Drug Administration Nonclinical studies Clinical trial Pharmacology Pharmaceutical sciences Research
98	EXTREME V GLUZIN™ When You Need Zinc – Choose Gluzin™ PURITY YOU CAN TRUST You understand the importance of zinc is vital for your health, and non-compliance is an ongoing problem for many of us. Generally, three f Add to Reading List Source URL: www.gluzin.com Language: English - Date: 2010-02-05 14:45:31 Food science Dietary minerals Dietary supplements Zinc compounds Zinc Human nutrition Excipient Dietary Reference Intake Zinc toxicity Chemistry Nutrition Matter
99	Quality Challenges and Research Needs in the Generic Pharmaceutical Industry GDUFA Regulatory Science Initiatives Public Meeting June 21, 2013 Silver Spring, MD Add to Reading List Source URL: www.fda.gov Language: English Clinical research Food and Drug Administration Excipient Packaging and labeling Biosimilar Generic drug Xcelience NIPTE Pharmaceutical sciences Pharmacology Pharmaceutical industry
100	Provisional Translation PREFACE The 16th Edition of the Japanese Pharmacopoeia (JP) was promulgated by Ministerial Notification No. 65 of the Ministry of Health, Labour and Welfare Add to Reading List Source URL: www.pmda.go.jp Language: English - Date: 2014-04-23 21:04:28 Alcohols Dosage forms Euphoriants Pharmaceutical industry Tablet Morphine Starch Excipient Tramadol Chemistry Pharmacology Pharmaceutical sciences

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